US4333991A - Magnetic garnet film and manufacturing method therefor - Google Patents
Magnetic garnet film and manufacturing method therefor Download PDFInfo
- Publication number
- US4333991A US4333991A US06/258,005 US25800581A US4333991A US 4333991 A US4333991 A US 4333991A US 25800581 A US25800581 A US 25800581A US 4333991 A US4333991 A US 4333991A
- Authority
- US
- United States
- Prior art keywords
- film
- garnet film
- magnetic
- feal
- substrate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000002223 garnet Substances 0.000 title claims abstract description 68
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 53
- 238000004519 manufacturing process Methods 0.000 title description 6
- 229910015372 FeAl Inorganic materials 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 20
- 239000000758 substrate Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 20
- 239000013078 crystal Substances 0.000 claims description 13
- 230000008569 process Effects 0.000 claims description 7
- 238000000407 epitaxy Methods 0.000 claims 2
- 239000004973 liquid crystal related substance Substances 0.000 claims 2
- 239000010408 film Substances 0.000 description 80
- 239000010409 thin film Substances 0.000 description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 11
- 230000003287 optical effect Effects 0.000 description 10
- 239000000463 material Substances 0.000 description 8
- 238000004943 liquid phase epitaxy Methods 0.000 description 7
- 239000004065 semiconductor Substances 0.000 description 6
- 230000005374 Kerr effect Effects 0.000 description 4
- 229910016629 MnBi Inorganic materials 0.000 description 4
- 229910052797 bismuth Inorganic materials 0.000 description 4
- 230000005381 magnetic domain Effects 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000005415 magnetization Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000005300 metallic glass Substances 0.000 description 3
- 229910052761 rare earth metal Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 229910052688 Gadolinium Inorganic materials 0.000 description 2
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 2
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000010355 oscillation Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- 229910005543 GaSe Inorganic materials 0.000 description 1
- 229910000530 Gallium indium arsenide Inorganic materials 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229910052772 Samarium Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JSUSQWYDLONJAX-UHFFFAOYSA-N iron terbium Chemical compound [Fe].[Tb] JSUSQWYDLONJAX-UHFFFAOYSA-N 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000005404 monopole Effects 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F10/00—Thin magnetic films, e.g. of one-domain structure
- H01F10/08—Thin magnetic films, e.g. of one-domain structure characterised by magnetic layers
- H01F10/10—Thin magnetic films, e.g. of one-domain structure characterised by magnetic layers characterised by the composition
- H01F10/18—Thin magnetic films, e.g. of one-domain structure characterised by magnetic layers characterised by the composition being compounds
- H01F10/20—Ferrites
- H01F10/24—Garnets
- H01F10/245—Modifications for enhancing interaction with electromagnetic wave energy
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B19/00—Liquid-phase epitaxial-layer growth
- C30B19/02—Liquid-phase epitaxial-layer growth using molten solvents, e.g. flux
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/16—Oxides
- C30B29/22—Complex oxides
- C30B29/28—Complex oxides with formula A3Me5O12 wherein A is a rare earth metal and Me is Fe, Ga, Sc, Cr, Co or Al, e.g. garnets
Definitions
- the present invention relates to a magnetic garnet film used for photomagnetic recording and, more particularly, to a bismuth/rare earth/ferrogarnet film having a rectangular hysteresis characteristic.
- a ferromagnetic thin film such as a magnetic garnet film
- a recording medium using a magnetic thin film is disclosed as the prior art of such a magnetic recording medium in the Japanese Patent Disclosure No. 31703/77. This public disclosure involves the case wherein an amorphous Tb-Fe (terbium-iron) film is used.
- the Tb-Fe film has a large and stable coercive force near room temperature and has a low Curie temperature of about 150° C. This film is thus advantageous in that it requires only a little energy for writing of data.
- a Tb-Fe film as shown in this disclosed publication readout of the data by the Faraday effect, utilizing the rotation of the deflection plane of transmitted light, is almost impossible, since the optical figure of merit of the Tb-Fe film is extremely low. For this reason, the Kerr effect, utilizing the rotation of the deflection plane of reflected light, is used.
- the Kerr rotation angle ⁇ k in this case is as small as 0.3°; it is thus very difficult to obtain a high S/N ratio (signal to noise ratio) during data readout.
- S/N ratio signal to noise ratio
- the Tb-Fe film presents the problem of stability of the material, in terms of oxidation, crystallization, and mechanical strength, etc.
- Tb-Fe film instead of the Tb-Fe film as disclosed in the said publication and as described above, utilization of polycrystalline metal thin films such as MnBi (manganese/bismuth) or amorphous thin films such as GdFe (gadolinium/iron) has been conventionally proposed.
- magnetic thin film material such as MnBi has a high Curie temperature and thus requires much energy for writing of data.
- Amorphous metal thin films such as GdFe have practical problems of insufficient stability against oxidation, crystallization and the like.
- polycrystalline metal thin films such as MnBi and amorphous metal thin films such as GdCo, GdFe, and TbFe have inferior optical utility efficiency.
- this region is irradiated by a laser beam polarized by a polarizer, and the data is read out utilizing the magnetic Kerr effect according to which the angle of polarization or deflection of the reflected light varies in compliance with the magnetization condition. Since the transmittance of light is inferior with both of these thin films, readout of the data utilizing the Faraday effect is practically impossible. Since the Kerr rotation angle during readout of the data utilizing the Kerr effect is at most 0.3° to 0.4°, the S/N ratio cannot be made sufficiently high.
- the present inventor has conducted various experiments and studies to overcome these problems.
- a method has been established for controlling the photomagnetic characteristics (the wavelength dependency of the specific Faraday rotation, the absorption coefficient, and so on), the coercive force, the compensation temperature, the Curie temperature and so on by varying the kind and ratio of the rare earth elements in the magnetic thin film, the ratio of Bi substitution with respect to the rare earth elements, the crystal growing temperature, and so on.
- the present invention has been made in consideration of this and has for its object to provide a magnetic garnet film on which writing of data is possible with an electromagnetic wave having a wavelength within the visible range, and transmittal reading of the data at a high S/N ratio is possible with an electromagnetic wave having a wavelength in the near-infrared region.
- the present invention provides a magnetic garnet film having a composition represented by the chemical formula (BiGdLu) 3 (FeAl) 5 O 12 or (BiGdSm) 3 (FeAl) 5 O 12 .
- a practical semiconductor laser may be utilized for reading or writing (recording/reproducing). For example, it is possible to use an electromagnetic wave of 6,000 A wavelength (visible light) for recording, and an electromagnetic wave of 8,300 A wavelength (near-infrared light) for reproduction.
- the material for the practical semiconductor laser may include GaSe (with an oscillation wavelength of about 5,900 A), GaAs (about 8,300 to 9,100 A), and InGaAs (about 8,500 to 31,000 A).
- the magnetic garnet film of the above composition is transparent and has good optical characteristics. Thus, this film has a large absorption coefficient within the visible range, so writing of data is easy.
- the magnetic garnet film of the above composition has a rectangular hysteresis characteristic and exhibits good values of coercive force, compensation temperature, and Curie temperature, thereby providing an excellent digital recording medium.
- the magnetic garnet film of the above composition may be of multilayered structure (e.g., bi-layered) incorporating a photoelectric film such as a CdS film (cadmium sulfide). In this case, the energy required for writing the data is reduced in comparison with the case of the garnet film alone, thereby facilitating the writing of the data. It is also possible to write the data at the compensation temperature or at the Curie temperature.
- FIG. 1 is a graph showing the relationship between the growth temperature T growth (°C.) and the mismatch amount ⁇ a (A) of the lattice constant of the magnetic garnet film according to an embodiment of the present invention, which is formed on a Gd 3 Ga 5 O 12 (GGG) substrate by the liquid phase epitaxy method;
- FIG. 2 is a graph showing the relationship between the compensation temperature T comp (°C.) and the growth temperature T growth (°C.) of the magnetic garnet film shown in FIG. 1;
- FIG. 3 is a graph showing the relationship between the coercive force Hc(Oe) and the temperature (°C.) of the magnetic garnet film shown in FIG. 1;
- FIG. 4 is a graph showing the hysteresis characteristic of the magnetic garnet film corresponding to curve 12 of FIG. 3;
- FIG. 5 is view showing the magnetic pattern when printing is performed on the magnetic garnet film shown in FIG. 1.
- the magnetic garnet film of the present invention may be a single crystal, represented by the general chemical formula (BiGdLu) 3 (FeAl) 5 O 12 or (BiGdSm) 3 (FeAl) 5 O 12 .
- the following description will be made with reference to a magnetic garnet film having the composition (Bi 0 .3 Gd 2 .1 Lu 0 .6) 3 (Fe 4 .2 Al 0 .8) 5 O 12
- magnetic garnet films of other component ratios and the magnetic garnet film of the formula (BiGdSm) 3 (FeAl)5O 12 are also within the contemplated scope of the present invention.
- BiGdLu (or BiGdSm) will hereinafter be referred to as R for brevity.
- a magnetic garnet film R 3 (FeAl) 5 O 12 according to the present invention is grown on a Gd 3 Ga 5 O 12 (GGG) substrate by the liquid phase epitaxial growth method or the liquid phase epitaxy method (LPE method). Since this LPE method is generally known, the description thereof will be omitted.
- FIG. 1 shows the relationship between the growth temperature T growth (°C.) and the mismatch amount ⁇ a (A) of the lattice constant when the garnet thin film is formed on the substrate by the LPE method as mentioned above.
- Curve 10 represents the case wherein the substrate was rotated while the film was being formed by the LPE method
- curve 12 represents the case wherein the substrate was not rotated.
- the mismatch amount ⁇ a may be represented as af-as, where "as” is the lattice constant of the substrate and “af” is the lattice constant of the garnet film. From FIG. 1, it is seen that the mismatch amount ⁇ a decreases in inverse proportion to the growth temperature T growth .
- the lattice constant "af” increases as the amount of substitution of Bi in the term R increases, and the lattice constant "af” decreases as the amount of Al in the term (FeAl) increases. This is attributable to the fact that the Bi atom is relatively large and the Al atom is relatively small.
- the mismatch amount ⁇ a may be adjusted to a desired value by incorporating a suitable amount of Al in the garnet film.
- Bi which increases the lattice constant of the R 3 (FeAl) 5 O 12 type film, more readily enters the material as the growth temperature T growth is lowered, and Al less readily enters the material as T growth is lowered.
- Bi also functions to lower the saturation magnetization 4 ⁇ Ms of the film.
- the mismatch amount ⁇ a may be suitably varied depending upon the composition of the garnet film, the crystal growth conditions, the required magnetic optical characteristics and so on. However, when taking the composition (Bi 0 .3 Gd 2 .1 Lu 0 .6) 3 (Fe 4 .2 Al 0 .8) 5 O 12 as an example, the mismatch amount ⁇ a as shown in FIG. 1 is suitable. Furthermore, as shown in FIG. 1, the mismatch amount ⁇ a may be made larger when the substrate is rotated (10) than the case wherein the substrate is not rotated (12) at the same temperature.
- FIG. 2 shows the relationship between the compensation temperature T comp (°C.) of the R 3 (FeAl) 5 O 12 garnet film of the composition described above and the growth temperature T growth (°C.) of the garnet film formed by the LPE method.
- curve 10 represents the case wherein the GGG substrate was rotated during growth of the crystals
- curve 12 represents the case wherein the substrate was not rotated. From FIG. 2, it is seen that the compensation temperature T comp increases substantially in proportion to the growth temperature T growth . It can thus be seen from FIGS.
- FIG. 3 shows the relationship between the coercive force Hc (Oe) and the film temperature (°C.) of the garnet film of the composition described above.
- the coercive force Hc has a singular point, that is, the maximum value of Hc with respect to the temperature T, and that this Hc characteristic varies depending on whether or not the substrate is rotated during the growth process of the crystals.
- the singular point (compensation temperature) is high and is substantially at room temperature when the substrate is not rotated (12). This compensation temperature is lowered when the substrate is rotated (10).
- the compensation temperature may be freely controlled within the range of about -20° to +35° C. by suitably varying the growth temperature T growth and/or the content of gadolinium Gd in the garnet film.
- FIG. 4 shows the hysteresis characteristic of a garnet film at 24° C. for the case of curve 12 of FIG. 3.
- the coercive force in this case is about 230 Oe and shows a good rectangular hysteresis characteristic.
- Sm may be substituted for the element Lu in the chemical formula (BiGdLu) 3 (Fe Al ) 5 O 12 .
- the coercieve force of the film can be made about 430 Oe.
- the substrate for growing the garnet film thereon may be made of Sm 3 Ga 5 O 12 (SmGG) or Nd 3 Ga 5 O 12 (NdGG).
- the Faraday rotation angle of the garnet film having the characteristics as shown in FIGS. 3 and 4 was measured to be 0.63 ⁇ 10 4 deg/cm for the laser beam of 6,328 A wavelength.
- the film thickness of this garnet film was easily controllable within the range of about 0.5 ⁇ m to about 3 ⁇ m. With a garnet film of 3 ⁇ m thickness, a Faraday rotation angle of about 2° at the deflection plane is obtainable. This is a considerably better value than the Kerr rotation angle (about 0.3°) of the prior art amorphous magnetic thin film described above.
- an improvement of about 16 dB in the S/N ratio may be realized. This indicates that an improvement of about 16 dB noise margin is possible for digital signal processing.
- the figure of merit of the garnet film according to this example of the present invetnion is about b 5 degree/dB at 6,000 A wavelength, about 900 degree/dB at 11,000 A wavelength.
- the figure of merit (degree/dB) as described above is defined as the ratio of the Faraday rotation angle (degree) to the absorption constant (dB) and represents the practical standard for utilizing the Faraday effect in practice.
- a laser beam of a suitable wavelength is used considering the figure of merit described above.
- writing is performed with a laser beam of relatively short wavelength and reading is performed with a laser beam of relatively long wavelength.
- a monopole magnetic head for writing and a laser beam of relatively long wavelength for reading out the data.
- Various semiconductor materials for semiconductor lasers are known which provide various laser beam wavelengths. For example, a ZnS laser has an oscillation wavelength of about 3,300 A and a PbSnSe laser provides a laser beam of about 80,000 to 312,000 A wavelength.
- FIG. 5 shows an example of a data pattern printed from a recorded magnetic tape as observed with a vertical illuminating type polarizing microscope.
- the printed pattern is observed utilizing the Kerr effect with a reflex type polarizing microscope.
- the printed pattern shown in FIG. 5 shows great contrast, and the garnet film according to the present invention is confirmed to have superior optical characteristics.
- the present inventor selected some of the garnet films having substantially the same characteristics as those of FIGS. 3 and 4 and measured the Curie temperature.
- the Curie temperature of these garnet films was confirmed to be about 180° C. This Curie temperature may further be lowered by varying the content of Al (component ratio within the composition) of the garnet films.
- This Curie temperature, 180° C. is considerably lower than the Curie temperature of the MnBi film (about 360° C.) It is seen from this that the energy required for writing data may be made smaller.
- the growth process technique of the substrate has been perfected and it has become easy to manufacture a GGG substrate without lattice defects.
- the material cost of the substrate becomes higher as compared with semiconductor elements, the manufacturing process is, on the other hand, easier. From the overall point of view, the garnet film of the present invention presents sufficient advantages for mass production.
- the magnetic garnet film according to the present invention is not only suitable for mass production but has advantageous optical characteristics over the conventional materials of the same type in that it is transparent and has a large angle of polarization or deflection and also writing of data is possible with a relatively low energy.
- the garnet film according to the present invention may also be applied to a magnetic bubble memory device or the like.
- cylindrical magnetic domains or bubble magnetic domains may be formed within the film by applying a vertical bias magnetic field Hb of a suitable magnitude to the surface of the film under the condition Is/ ⁇ o ⁇ Ha where Ha (A/m) is the magnetic anisotropy of the garnet film and Is is the spontaneous magnetization.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Metallurgy (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Power Engineering (AREA)
- Thin Magnetic Films (AREA)
- Compounds Of Iron (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
Abstract
Description
Claims (9)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP55-58400 | 1980-05-01 | ||
JP5840080A JPS56155515A (en) | 1980-05-01 | 1980-05-01 | Magnetic garnet film and manufacture |
Publications (1)
Publication Number | Publication Date |
---|---|
US4333991A true US4333991A (en) | 1982-06-08 |
Family
ID=13083302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US06/258,005 Expired - Lifetime US4333991A (en) | 1980-05-01 | 1981-04-27 | Magnetic garnet film and manufacturing method therefor |
Country Status (4)
Country | Link |
---|---|
US (1) | US4333991A (en) |
EP (1) | EP0039463B1 (en) |
JP (1) | JPS56155515A (en) |
DE (1) | DE3164124D1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4544239A (en) * | 1983-03-16 | 1985-10-01 | Litton Systems, Inc. | Compressed bismuth-containing garnet films of replicable low anisotropy field value and devices utilizing same |
US4622264A (en) * | 1982-10-20 | 1986-11-11 | Hitachi, Ltd. | Garnet film for magnetic bubble memory element |
US4625390A (en) * | 1983-03-16 | 1986-12-02 | Litton Systems, Inc. | Two-step method of manufacturing compressed bismuth-containing garnet films of replicable low anisotropy field value |
US20030128418A1 (en) * | 2001-12-25 | 2003-07-10 | Tdk Corporation | Hard magnetic garnet material, faraday rotator, optical device, optical communication system, method of manufacturing faraday rotator and method of manufacturing bismuth-substituted rare earth iron garnet single crystal |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0129605A4 (en) * | 1982-12-23 | 1987-01-22 | Sony Corp | Thermomagnetic optical recording method. |
JPS61222109A (en) * | 1985-03-27 | 1986-10-02 | Nippon Sheet Glass Co Ltd | Manufacture of rare earth iron garner film |
JPH0354198A (en) * | 1989-07-20 | 1991-03-08 | Shin Etsu Chem Co Ltd | Oxide garnet single crystal |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3281363A (en) * | 1963-07-10 | 1966-10-25 | Bell Telephone Labor Inc | Bismuth-containing garnets and their preparation |
US3479292A (en) * | 1965-12-20 | 1969-11-18 | Bell Telephone Labor Inc | Manufacture of garnet ceramic |
US3654162A (en) * | 1970-10-01 | 1972-04-04 | Gte Laboratories Inc | Ferrimagnetic iron garnet having large faraday effect |
US3764195A (en) * | 1972-02-02 | 1973-10-09 | Bell Telephone Labor Inc | Optical waveguide devices using single-crystal garnet films |
US3838450A (en) * | 1972-01-08 | 1974-09-24 | Philips Corp | Thermomagnetic recording and magneto-optic reading of a medium having bismuth ions in a garnet structure |
DE2418711A1 (en) * | 1973-04-18 | 1974-10-31 | Hitachi Ltd | Single crystals of bismuth rare-earth garnets - lead-free bismuth gadolinium iron garnets with high faraday effect |
US3989352A (en) * | 1973-04-26 | 1976-11-02 | U.S. Philips Corporation | Bismuth substituted rare earth garnets as magneto-optic materials exhibiting magnetic circular dichroism |
US4256531A (en) * | 1977-08-09 | 1981-03-17 | National Institute For Researches In Inorganic Materials | Process for producing single crystal of yttrium-iron garnet or solid solution thereof |
US4293371A (en) * | 1980-03-27 | 1981-10-06 | Union Carbide Corporation | Method of making magnetic film-substrate composites |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1050862A (en) * | 1973-10-04 | 1979-03-20 | Richard E. Novak | Magnetic bubble devices and garnet films therefor |
-
1980
- 1980-05-01 JP JP5840080A patent/JPS56155515A/en active Pending
-
1981
- 1981-04-27 EP EP81103151A patent/EP0039463B1/en not_active Expired
- 1981-04-27 US US06/258,005 patent/US4333991A/en not_active Expired - Lifetime
- 1981-04-27 DE DE8181103151T patent/DE3164124D1/en not_active Expired
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3281363A (en) * | 1963-07-10 | 1966-10-25 | Bell Telephone Labor Inc | Bismuth-containing garnets and their preparation |
US3479292A (en) * | 1965-12-20 | 1969-11-18 | Bell Telephone Labor Inc | Manufacture of garnet ceramic |
US3654162A (en) * | 1970-10-01 | 1972-04-04 | Gte Laboratories Inc | Ferrimagnetic iron garnet having large faraday effect |
US3838450A (en) * | 1972-01-08 | 1974-09-24 | Philips Corp | Thermomagnetic recording and magneto-optic reading of a medium having bismuth ions in a garnet structure |
US3764195A (en) * | 1972-02-02 | 1973-10-09 | Bell Telephone Labor Inc | Optical waveguide devices using single-crystal garnet films |
DE2418711A1 (en) * | 1973-04-18 | 1974-10-31 | Hitachi Ltd | Single crystals of bismuth rare-earth garnets - lead-free bismuth gadolinium iron garnets with high faraday effect |
US3989352A (en) * | 1973-04-26 | 1976-11-02 | U.S. Philips Corporation | Bismuth substituted rare earth garnets as magneto-optic materials exhibiting magnetic circular dichroism |
US4256531A (en) * | 1977-08-09 | 1981-03-17 | National Institute For Researches In Inorganic Materials | Process for producing single crystal of yttrium-iron garnet or solid solution thereof |
US4293371A (en) * | 1980-03-27 | 1981-10-06 | Union Carbide Corporation | Method of making magnetic film-substrate composites |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4622264A (en) * | 1982-10-20 | 1986-11-11 | Hitachi, Ltd. | Garnet film for magnetic bubble memory element |
US4544239A (en) * | 1983-03-16 | 1985-10-01 | Litton Systems, Inc. | Compressed bismuth-containing garnet films of replicable low anisotropy field value and devices utilizing same |
US4625390A (en) * | 1983-03-16 | 1986-12-02 | Litton Systems, Inc. | Two-step method of manufacturing compressed bismuth-containing garnet films of replicable low anisotropy field value |
US20030128418A1 (en) * | 2001-12-25 | 2003-07-10 | Tdk Corporation | Hard magnetic garnet material, faraday rotator, optical device, optical communication system, method of manufacturing faraday rotator and method of manufacturing bismuth-substituted rare earth iron garnet single crystal |
US6775052B2 (en) * | 2001-12-25 | 2004-08-10 | Tdk Corporation | Hard magnetic garnet material, faraday rotator, optical device, optical communication system, method of manufacturing faraday rotator and method of manufacturing bismuth-substituted rare earth iron garnet single crystal |
Also Published As
Publication number | Publication date |
---|---|
EP0039463B1 (en) | 1984-06-13 |
EP0039463A1 (en) | 1981-11-11 |
JPS56155515A (en) | 1981-12-01 |
DE3164124D1 (en) | 1984-07-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS5873746A (en) | Photomagnetic recording medium | |
US5747136A (en) | High-density magneto-optic disk and method of manufacturing the same | |
Abe et al. | Magneto-optical recording on garnet films | |
GB2071696A (en) | Magneto-optical Recording Medium | |
JPH0118506B2 (en) | ||
US4701881A (en) | Magneto-optical recording medium | |
JPH0249002B2 (en) | ||
US4152486A (en) | Magneto-optical memory medium | |
US4814238A (en) | Magneto-optical recording medium | |
JPS6227459B2 (en) | ||
US4333991A (en) | Magnetic garnet film and manufacturing method therefor | |
US4612068A (en) | Magneto-optical recording medium | |
US5660929A (en) | Perpendicular magnetic recording medium and method of producing same | |
JPS6115308A (en) | magneto-optical recording material | |
US4695514A (en) | Magneto-optical memory element | |
US6086993A (en) | Magneto-optical recording medium | |
Buschow | Magneto-optical recording materials | |
US5391431A (en) | Magneto-optical recording medium | |
CA1216941A (en) | Thermo-magnetic recording materials supporting small stable domains | |
JPS60187954A (en) | Magnetic recording medium consisting of thin magnetic film | |
US5529854A (en) | Magneto-optic recording systems | |
Zeper et al. | Co/Pt multilayers for magneto‐optical recording | |
Gambino | Magneto-optical recording materials-past, present and future | |
JPS5873030A (en) | Optical magnetic recording medium | |
JPH0465523B2 (en) |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: OLYMPUS OPTICAL CO., LTD., 43-2, 2-CHOME, HATAGAYA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:SAKURAI YOSHIFUMI;REEL/FRAME:003881/0604 Effective date: 19810415 |
|
STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YEAR, PL 96-517 (ORIGINAL EVENT CODE: M170); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY Year of fee payment: 4 |
|
FEPP | Fee payment procedure |
Free format text: PAYMENT IS IN EXCESS OF AMOUNT REQUIRED. REFUND SCHEDULED (ORIGINAL EVENT CODE: F169); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 8TH YEAR, PL 96-517 (ORIGINAL EVENT CODE: M171); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY Year of fee payment: 8 |
|
REFU | Refund |
Free format text: REFUND - PAYMENT OF MAINTENANCE FEE, 8TH YEAR, PL 96-517 (ORIGINAL EVENT CODE: R171); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
FEPP | Fee payment procedure |
Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 12TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M185); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY Year of fee payment: 12 |